Browse through 1,540 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Zimmer, Inc. recalled the Affixus Antegrade Femoral Nail on December 2, 2025, due to a risk of fatigue fractures. The recall affects three units distributed nationwide across several states. Patients should stop using the device immediately and consult healthcare providers for further instructions.
Zimmer recalled 11 Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may fracture, leading to serious health risks. Patients should stop using the device immediately and follow manufacturer instructions.
Zimmer recalled 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized distal diameter, risking fatigue fractures. This can lead to serious health complications requiring surgical intervention.
Microbiologics recalled 86 units of the KWIK-STIK 2-Pack on December 2, 2025. The affected products may fail to recover the target microorganism Campylobacter jejuni. This recall affects units distributed worldwide, including the U.S.
Zimmer Inc. recalled 23 units of the Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may have an undersized distal diameter, leading to potential health risks. Patients should stop using the devices immediately and contact their healthcare provider.
Affixus recalled 22 units of its antegrade femoral nailing system on December 2, 2025, due to a risk of implant fatigue fracture. The defect may lead to serious health complications including tissue damage and pain. Consumers and healthcare providers must stop using the affected implants immediately.
Zimmer, Inc. recalled 23 units of the Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized distal diameter, risking implant fatigue fracture. This defect can cause severe health issues, including pain and tissue damage requiring surgery.
Affixus recalled its Antegrade Femoral Nailing System on December 2, 2025, due to a potential implant fatigue fracture risk. The recall affects 22 units distributed nationwide in 14 states. Patients should stop using the affected devices immediately to avoid serious health risks.
Zimmer Inc. recalled 24 Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may have undersized distal diameters, leading to potential fractures. Users should stop using the product immediately and contact their healthcare provider.
Zimmer Inc. recalled 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have undersized distal diameters, risking implant fatigue fractures. Consumers should stop using the device immediately and follow manufacturer instructions.
Zimmer recalled 24 Affixus Antegrade Femoral Nails on December 2, 2025, due to a risk of implant fatigue fracture. Affected implants may cause serious health issues, including tissue damage and pain. Healthcare providers must stop using the device immediately and follow recall instructions.
Zimmer issued a recall for 22 Affixus Antegrade Femoral Nails on December 2, 2025. The implants may have an undersized diameter, risking fatigue fractures. This defect could lead to severe health complications for patients.
Mondelez Global recalled 70 cases of Ritz Peanut Butter Cracker Sandwiches on November 28, 2025. The recall stems from undeclared peanut allergens due to mispackaging. The affected product was distributed in eight states including Alabama and New York.
Ebern Designs recalled Ojaswi 12-Drawer Dressers on November 26, 2025, due to a tip-over and entrapment hazard. The dressers can cause serious injuries or death if not anchored to the wall. Consumers should stop using the dressers immediately and contact the company for a refund.
Ikuso recalled safety gates on November 26, 2025, due to a serious entrapment risk. The gates can allow a child’s torso to fit through, violating mandatory safety standards. Consumers should stop using the gates immediately and seek a refund.
KingPavonini recalled six models of adult portable bed rails due to serious risks of entrapment and asphyxiation. The recall affects products sold on Amazon since November 2025. Consumers must stop using these bed rails immediately and seek a refund or replacement.
Winder Laboratories, LLC recalled 3,528 bottles of Morphine Sulfate Oral Solution on November 26, 2025. The labeling error misrepresented the product size, leading to potential dosing issues. Consumers should stop using the product immediately and consult their healthcare provider.
Rotinyard recalled convertible high chairs on November 26, 2025, due to fall and entrapment hazards. The recalled chairs lack the required restraint system, posing serious risks to infants. Consumers should stop using these products immediately and seek a refund.
Macardac recalled baby loungers on November 26, 2025, due to serious risks of entrapment and falls. The loungers violate safety standards for infant products. Consumers should stop using the loungers immediately and seek a refund.
Alinux recalled its baby loungers on November 26, 2025, due to serious injury or death risks from entrapment and fall hazards. The loungers do not comply with mandatory safety standards for infant sleep products. Consumers should stop using them immediately and seek a refund.